Ձեր նորածնի գենետիկ առողջության ավելի լիարժեք պատկերը

Conditions related to enzyme deficiencies or substrate buildup. Early detection enables dietary modifications and enzyme replacement therapy.

Inherited disorders causing severe defects in T and B cells. Treatable with antibiotics and stem cell transplantation when caught early.

Complex disorders including kidney disease, muscular conditions, and respiratory conditions.

Early-onset hearing loss genes. Early identification enables intervention before speech development is impacted.

Genes associated with cancers that can develop in early childhood. Enables increased surveillance and screening.

Abnormal development of red blood cells or blood vessels leading to anemia, hemorrhaging, or hemolysis.

Neurological disorders causing seizures. Early detection enables routine monitoring and medication.

Congenital heart defects involving walls, valves, arteries, and veins of the heart.

Conditions affecting vision that can impact a child’s growth and development.